Evaluation of Vitrectomy for Diabetic Macular Edema (Vitrectomy-D)
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Purpose
The study is designed as a prospective cohort study to assess changes in visual acuity and retinal thickening and surgical complications in subjects undergoing vitrectomy for diabetic macular edema.
The study also aims to identify subgroups in which there appears to be a benefit of vitrectomy and subgroups in which vitrectomy does not appear to be beneficial and to obtain data that can be used to plan a randomized trial.
Subject will be followed through 2 years, with a primary outcome at 6 months post vitrectomy surgery. The vitrectomy procedure will be performed based on the investigators usual care and is not considered part of the research although the procedure performed will be collected.
| Condition |
|---|
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Diabetic Retinopathy Diabetic Macular Edema |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Evaluation of Vitrectomy for Diabetic Macular Edema Study |
- Visual Acuity [ Time Frame: Baseline to 6 months ] [ Designated as safety issue: No ]Change in best correct visual acuity letter score from baseline to one year as measured by a certified tester using an electronic visual acuity testing machine based on the Early Treatment Diabetic Retinopathy Study (ETDRS) method. A positive change denotes an improvement. Best value on the scale 97, worst 0.
- Change in Optical Coherence Tomography Measured Central Subfield Thickness From Baseline [ Time Frame: Baseline to 6 Months ] [ Designated as safety issue: No ]Change in central subfield thickness is followup central subfield retinal thickness minus baseline thickness.
- Percent of Participants With Change in Visual Acuity From Baseline to Six Months [ Time Frame: Baseline to 6 months ] [ Designated as safety issue: No ]
- Change in Optical Coherence Tomography Central Subfield Thickness From Baseline to 6 Months [ Time Frame: Baseline to 6 months ] [ Designated as safety issue: No ]Change in thickness is followup thickness minus baseline thickness.
- Surgical Complications From Baseline to Six Months [ Time Frame: Baseline to 6 months ] [ Designated as safety issue: Yes ]Including intraoperative and perioperative medical complications. Same subject could have more than one complication
| Enrollment: | 87 |
| Study Start Date: | July 2005 |
| Study Completion Date: | February 2009 |
| Primary Completion Date: | August 2008 (Final data collection date for primary outcome measure) |
| Groups/Cohorts |
|---|
|
Primary
Subjects vitreomacular traction, visual acuity 20/63 to 20/400, retinal thickness >300 microns in the central subfield on OCT, and cataract extraction not being performed in conjunction with vitrectomy.
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Show Detailed Description
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
adults with diabetic macular edema
Subject-level Inclusion Criteria
To be eligible, the following inclusion criteria (1-3) must be met:
- Age >= 18 years
- Diagnosis of diabetes mellitus (type 1 or type 2)
Able and willing to provide informed consent.
Subject-level Exclusion Criteria
A patient is not eligible if any of the following exclusion criteria (4-6) are present:
- A condition that, in the opinion of the investigator, would preclude participation in the study (e.g., unstable medical status including blood pressure and glycemic control).
- Patient is expecting to move out of the area of the clinical center to an area not covered by another clinical center during the first year of the study.
- Blood pressure >180/110 (systolic above 180 OR diastolic above 110).
Study Eye Criteria
To be a study eye, all of the inclusion criteria (a-e) and none of the exclusion criteria (f-m) listed below must be met. A patient can have only one study eye. If both eyes are eligible and undergoing vitrectomy, the first eye having surgery will be the study eye.
The eligibility criteria for a study eye are as follows:
Inclusion
- Vitrectomy being performed as treatment for DME.
- E-ETDRS visual acuity 20/800 or better (E-ETDRS visual acuity score >= 3 letters).
- Definite retinal thickening due to diabetic macular edema based on clinical exam involving the center of the macula.
- Presence of vitreomacular traction associated with macular edema OR edema is felt to be too diffuse to respond to focal or grid laser OR edema judged to be inadequately responsive to previous treatment(s) and unlikely to benefit from further focal photocoagulation.
Media clarity, pupillary dilation, and patient cooperation sufficient for adequate fundus photographs.
Exclusion
- Macular edema is considered to be due to a cause other than diabetic macular edema.
- An ocular condition is present such that, in the opinion of the investigator, visual acuity would not improve from resolution of macular edema (e.g., foveal atrophy, pigmentary abnormalities, subfoveal hard exudates, fibrous metaplasia, nonretinal condition).
- An ocular condition is present (other than diabetes) that, in the opinion of the investigator, might affect macular edema or alter visual acuity during the course of the study (e.g., vein occlusion, uveitis or other ocular inflammatory disease, neovascular glaucoma, post-surgical cystoid macular edema, etc.).
- History of retinal macular photocoagulation, intravitreal corticosteroids, or other treatment for DME within 3.5 months prior to enrollment.
- History of peripheral scatter photocoagulation within 4 months prior to enrollment or anticipated need within the 4 months following enrollment.
- History of prior pars plana vitrectomy.
- History of major ocular surgery (including cataract extraction, scleral buckle, any intraocular surgery, etc.) within prior 6 months or anticipated within the next 6 months following enrollment.
- History of YAG capsulotomy performed within 2 months prior to enrollment.
Contacts and Locations
Hide Study Locations| United States, California | |
| University of California, Irvine | |
| Irvine, California, United States, 92697 | |
| Loma Linda University Health Care, Dept. of Ophthalmology | |
| Loma Linda, California, United States, 92354 | |
| Southern California Desert Retina Consultants, MC | |
| Palm Springs, California, United States, 92262 | |
| West Coast Retina Medical Group, Inc. | |
| San Francisco, California, United States, 94107 | |
| Bay Area Retina Associates | |
| Walnut Creek, California, United States, 94598 | |
| United States, Florida | |
| University of Florida College of Med., Department of Ophthalmology | |
| Jacksonville, Florida, United States, 32209 | |
| Florida Retina Consultants | |
| Lakeland, Florida, United States, 33805 | |
| Sarasota Retina Institute | |
| Sarasota, Florida, United States, 34239 | |
| Center for Retina and Macular Disease | |
| Winter Haven, Florida, United States, 33880 | |
| United States, Hawaii | |
| Retina Consultants of Hawaii, Inc. | |
| Aiea, Hawaii, United States, 96701 | |
| Retina Associates of Hawaii, Inc. | |
| Honolulu, Hawaii, United States, 96813 | |
| United States, Indiana | |
| Raj K. Maturi, M.D., P.C. | |
| Indianapolis, Indiana, United States, 46290 | |
| John-Kenyon American Eye Institute | |
| New Albany, Indiana, United States, 47150 | |
| United States, Kentucky | |
| Paducah Retinal Center | |
| Paducah, Kentucky, United States, 42001 | |
| United States, Maryland | |
| Elman Retina Group, P.A. | |
| Baltimore, Maryland, United States, 21237 | |
| Wilmer Eye Institute at Johns Hopkins | |
| Baltimore, Maryland, United States, 21287-9277 | |
| Retina Consultants of Delmarva, P.A. | |
| Salisbury, Maryland, United States, 21801 | |
| United States, Massachusetts | |
| Joslin Diabetes Center | |
| Boston, Massachusetts, United States, 02215 | |
| United States, Michigan | |
| Henry Ford Health System, Dept of Ophthalmology and Eye Care Services | |
| Detroit, Michigan, United States, 48202 | |
| Vitreo-Retinal Associates | |
| Grand Rapids, Michigan, United States, 49525 | |
| Associated Retina Consultants | |
| Williamsburg, Michigan, United States, 49690 | |
| United States, Minnesota | |
| Retina Center, PA | |
| Minneapolis, Minnesota, United States, 55404 | |
| University of Minnesota | |
| Minneapolis, Minnesota, United States, 55455 | |
| United States, Missouri | |
| Barnes Retina Institute | |
| St. Louis, Missouri, United States, 63110 | |
| United States, New York | |
| Retina Consultants, PLLC | |
| Slingerlands, New York, United States, 12159 | |
| Retina-Vitreous Surgeons of Central New York, PC | |
| Syracuse, New York, United States, 13224 | |
| United States, North Carolina | |
| Charlotte Eye Ear Nose and Throat Assoc, PA | |
| Charlotte, North Carolina, United States, 28210 | |
| Horizon Eye Care, PA | |
| Charlotte, North Carolina, United States, 28211 | |
| United States, Ohio | |
| Retina Associates of Cleveland, Inc. | |
| Beachwood, Ohio, United States, 44122 | |
| United States, Oklahoma | |
| Dean A. McGee Eye Institute | |
| Oklahoma City, Oklahoma, United States, 73104 | |
| United States, Oregon | |
| Casey Eye Institute | |
| Portland, Oregon, United States, 97239 | |
| Retina Northwest, PC | |
| Portland, Oregon, United States, 97210 | |
| United States, South Carolina | |
| Carolina Retina Center | |
| Columbia, South Carolina, United States, 29223 | |
| Palmetto Retina Center | |
| Columbia, South Carolina, United States, 29169 | |
| United States, South Dakota | |
| Black Hills Regional Eye Institute | |
| Rapid City, South Dakota, United States, 57701 | |
| United States, Tennessee | |
| Southeastern Retina Associates, PC | |
| Kingsport, Tennessee, United States, 37660 | |
| Southeastern Retina Associates, P.C. | |
| Knoxville, Tennessee, United States, 37909 | |
| Vanderbilt University Medical Center | |
| Nashville, Tennessee, United States, 37232 | |
| United States, Texas | |
| West Texas Retina Consultants P.A. | |
| Abilene, Texas, United States, 79605 | |
| Retina Research Center | |
| Austin, Texas, United States, 78705 | |
| Texas Retina Associates | |
| Dallas, Texas, United States, 75231 | |
| Charles A. Garcia, PA & Associates | |
| Houston, Texas, United States, 77002 | |
| Retina and Vitreous of Texas | |
| Houston, Texas, United States, 77025 | |
| Texas Retina Associates | |
| Lubbock, Texas, United States, 79424 | |
| Valley Retina Institute | |
| McAllen, Texas, United States, 78503 | |
| United States, Utah | |
| Rocky Mountain Retina Consultants | |
| Salt Lake City, Utah, United States, 84107 | |
| United States, Washington | |
| University of Washington Medical Center | |
| Seattle, Washington, United States, 98195 | |
| United States, Wisconsin | |
| University of Wisconsin-Madison, Dept of Ophthalmology/Retina Service | |
| Madison, Wisconsin, United States, 53705 | |
| Study Chair: | Julia A. Haller, M.D. | Wills Eye Institute |
More Information
No publications provided by Diabetic Retinopathy Clinical Research Network
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Diabetic Retinopathy Clinical Research Network |
| ClinicalTrials.gov Identifier: | NCT00709319 History of Changes |
| Other Study ID Numbers: | NEI-125, U10EY018817-03, U10EY014229-07, U10EY014231-09 |
| Study First Received: | July 1, 2008 |
| Results First Received: | July 27, 2011 |
| Last Updated: | February 16, 2012 |
| Health Authority: | United States: Federal Government |
Keywords provided by Diabetic Retinopathy Clinical Research Network:
|
Diabetic retinopathy Diabetic macular edema dme vitrectomy |
Additional relevant MeSH terms:
|
Diabetic Retinopathy Edema Macular Edema Retinal Diseases Eye Diseases Diabetic Angiopathies Vascular Diseases |
Cardiovascular Diseases Diabetes Complications Diabetes Mellitus Endocrine System Diseases Signs and Symptoms Macular Degeneration Retinal Degeneration |
ClinicalTrials.gov processed this record on May 16, 2013